Regulatory Affairs Senior Consultant
- Full time
- Herts/Essex area
- Hybrid – 1 day per month minimum office based
- Excellent remuneration and benefits offered
My client is seeking a full time permanent member of staff to join their team at this exciting stage in their growth. The candidate will be able to provide high-quality regulatory advice and project management to Clients. The candidate will have some experience in technical advice and product development strategies. We are looking for an ambitious individual with excellent communication skills, capable of delivering Project Management training programmes to support the evolution of our team. This is an excellent opportunity to progress your career at a rapidly growing Regulatory Consultancy Practice and to play a key role in the development and mentoring of junior staff.
Key Objectives
- Provide project management and regulatory advice/services to clients in all areas of the development of human medicinal products
- Develop and lead project management training programmes to promote operational excellence
- Ensure delivery of project goals within agreed timelines, maintaining oversight of project budgets
- Lead meetings with internal and external stakeholders on matters related to any current and/or future projects, contracts, or new business opportunities
- Line manage individual contributors, and in so doing provide ongoing coaching and mentoring
- Mentor and train junior members of the consultancy team (including Consultant and Associate levels)
- Lead multi-jurisdiction programs of work and deliver consulting services
- Contribute to technical authorship and review of development regulatory documents
- Prepare and review written estimates, quotations, and contracts for Clients as required
Skills and Experience
- A high scientific calibre with a life science focused BSc (or equivalent). Ideally the candidate will have a project management qualification and post graduate qualifications (MSc, PhD etc)
- A minimum of 5 years of project management experience within regulatory in a pharmaceutical or service provider industry role
- Proven project management experience in a consulting environment
- A professional manner and presentable appearance for meeting customers/clients
- Ability to balance competing priorities and complete work within a set timeframe
- Ability to work in a proactive and autonomous manner as well as leading a global team
- Exemplary organisational skills with a high level of attention to detail
- Exemplary verbal communication and presentation skills in English
- High level of computer literacy and competency in MS Office programs
- Willingness to work flexible hours and travel for short periods, sometimes at short notice, within the UK or internationally
